Note: Descriptions are shown in the official language in which they were submitted.
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The invention concerns a method for stabilizing a superconductor of
the type having at least one core consisting entirely or partly of an inter_
metallic superconductive compound and which is provided with a sheath of an
alloy which contains an electrically normal conducting metAl and an element
of the compound in general and more particularly to a method of improving
stabilization in such a superconductor.
Superconductive intermetallic compounds of the type A3B, consisting
of two elements, for example, Nb3Sn or V3Ga, which have an A_15 crystal
structure exhibit very good superconductor properties being particularly
distinguished by a high critical magnetic field, a high transition temperature
and a high critical current density. As a result, they are particularly well
suited as*superconductors for superconducting coils used to generate strong
magnetic fields such as are needed for research purposes. Other possible
applications include superconducting magnets for the suspension guidance
of magnetic suspension railroads and the windings of electric machines.
Recently, ternary compounds such as niobium-aluminum-germanium (Nb3Alo 8GeO 2)
have also become of special interest. However, since these compounds are very
brittle, their manufacture in a fcrm suitable, for example, for use in magnet
coils presents considerable difficulties. Several methods of manufacturing
superconductors in the form of long wires or ribbons with, in patticular,
two_component intermetAllic compounds have been disclosed. These methods
aro used particularly for the manufacture of what are known as multi-core
conductors. Such conductors have wires, typically of Nb3Sn or V3Ga, arranged
in-a normal conducting matrix. In the known methods, a ductile element, in
wire form, of the compound to be prepared, e.g., a niobium or vanadium wire,
is surrounded with a sleeve of an alloy containing a ductile carrier metal
and the remaining eloments of the compound, e.g., a copper_tin alloy or a
copper_gaU ium alloy. In particular, a multiplicity of such wires are em-
beddod in a matrix of the alloy. The structure so obtained is then subjected
to cross ~ection reducing processing to obtain a long wire such as is re-
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quired for coils As a result the diameter of the wires, e g., niobium or
vanadium wire, for example, is reduced to a small value in the order of
magnitude of about 30 to 50 ~m or even less, which is desirable in view of
the superconduction properties of the conductor Through the cross-section
reducing processing attempts are also made to obtain the best possible
metallurgical bond between the wire and the surrounding matrix material of
the alloy without, howevcr, the occurrence of reactions which lead to embritt_
lement of the conductor After the cross_section reducing processing, the
conductor, consisting of one or more wires and the surrounding matrix material,
is subjected to a heat treatment such that the desired compound is formed by
a reaction of the wire material, i.e , the niobium or vanadium, for instance,
with the further element, contained in the surrounding matrix, of the comp_
ound, e.g" tin or gallium. In this process, the element contained in the
matrix diffuses into the wire material, which consists of the other element
of the compound, and reacts therewith forming a layer consisting of the
desired compound. (See German Offenlegungsschrift 2,044,660; 2,052,323;
2,105,828.)
A particular difficulty ~ith the known methods is that the matrLx
material containing the embedded cores, consisting of the carrier metal and
the remaining elements of the compound to be produced, is relatively difficult
to deform, particularly for higher concentrations of these elements.
~roposed methods are also known which overcome this problem. In
these methods one or more cores of a ductile element of the compound to be
produced, particularly niobium or vanadium, are embedded in a ductile m~trix
material, e.g., copper, silver or nickel, which contains, at most, on~y very
small amounts of the element of the compound to be produced. The structure
consisting of the cores and this matrix material can then be processed with_
out any intermediate anneal by a cross_section reaucing process, e.g., by
cold_drawing, into a thin wire which contains very thin cores of vanadium or
niobium. After the last cross-section reducing process step, the remaining
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elements of the compound to be produced, e.g., tin in the case of Nb3Sn, are
then applied to the matrix material. This is done by briefly immersing the
wire in a tin melt, so that a thin tin layer is formed on the matrix material,
or by evaporating a tin layer on the matrix material. Subsequently, a heat
treatment is performed, in which the elements of the compound to be produced,
which have been applied to the matrix material, are first diffused into the
matrix material and then through it, and then form the desired superconductive
compound through reaction with the cores (see ~Applied Physics Letters" vol.
20 (1972); pages 443 to 445; German Offenlegungsschrift 2,205,308).
However, in all these methods the cores of the superconductive int-
ermetallic compound are surrounded by a matrix material which gener~lly
consists of an alloy of an electrically highly normal conducting metal, ~uch
as copper, with an element of the intermetallic compound, e.g , gallium or
tin in the finished conductor. Such alloys, of course, have both poorer
electric conductivity and poorer thermal conductivity than, for instance,
pure copper. This has an adverse effect on the electrical stabilization of
the conductors. For good electrical stabilization it is desirable that the
superconducting cores have an envel~pe of metal with an electric and theDmal
conductiv~$y which is as high as possible so that it can carry the current
flowing through conductor in the event of a transition of the superconducting
cores to the normal conducting state if necessary and can transfer heat
produced in the conductor, due to jumps in the magnetic flux or, in the event
of a transistion into the normal conducting state, due to ohmic losses, to
the coolant currounding the conductor.
To improve the stabilization, it is therefore desirable to replace
tho poorly conducting alloy matrix of the superconductors with a matrix or
onvelope of a motal which i9 as pure as possible and which has high electric
and th*rmal conductivity. In a method known from the German Offenlegungss-
chrift 2,205,308 this is accomplished by at least partially removing the
copper_tin matrix from the Nb3Sn coros in an Nb3Sn multi_core conductor,
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after the heat treatment for generating the Nb3Sn layers, using a chemical
reaction or electrolytic anodic dissolution. Subsequently, the cores are
provided with a copper matrix by conducting them through a bath of molten
copper which is kept at a temperature of 1100 C in an inert atmosphere.
Such a method, however, is extremely expensive and requires great
care in the control of the process both in order not to damage the Nb3Sn
cores when dissolving the matrix, and to obtain reproducible results
It is an object of the present invention to stabilize a supercon-
ductor with at least one core which consists entirely or partly of an inter-
metallic superconductive compound and is provided with a sheath of an alloy
containing an electrically highly normal conducting metal and one element of
the compound in a considerably simpler manner.
With the present invcntion this is accomplished by at least
partially removing from the sheath the element of the compound contained
therein using a chemical transport reaction.
In accordance with~the present invention therefore, there is
provided a method for stabilizing a superconductor having at least one core
which consists at least partially of an intermetallic superconducti~e
compound of the type A3B~consisting of at least two elements and which is
; 20 provided with a sheath of an alloy containing an electrically highly normal
conducting metal and one element of the compound comprising: a. disposing
the superconductor and a gaseous transport agent within a vessel containing
no other active gases; b. heating said vessel to the po nt where a chemical
tranqport reaction takes place in whichhthe element of the compound in the
sheath reacts with the transport agent to form a gaseous reaction product,
and where at another point within the vessel a reverse reaction takes place
dcpositing the said element in said gaseous reaction product on another
surface within said vessel.
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Chemical transport reactions themselves are known and arecharacterized by the feature that a solid or liquid substance reacts with
gases, forming only gaseous reaction products, and that subsequently, at
other
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points of the system, a reverse reaction takes place, the starting substance
being precipitated. A condition for a chemical transport reaction is, besides
the reversibility of the chemical reaction that takes place, the presence of
a concentration gradient between the point at which the gaseous reaction
products are formed and the point where the reverse reaction through decompo-
sition of these reaction products is to take place ~see H. Schaefer, "Chemical
Transport Reactions", Weinheim/Bergstr., Verlag Chemie, 1962, page 11).
As compared to known methods, a large number of advantages are
obtained through the use of chemical transport reactions for removing there-
from with the present method the element of the compound contained in the
sheath. First, it has been found that chemical transport reactions can be
carried out at temperatures which are considerably below the melting point
~b
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of copper. In addition the separation of the matrix from the cores and, thus,
destruction of the good metallurgical contact of the cores with the matrix
material which was established during the cross_section-reducing processing
is avoided. Also, thè element contained in the sheath can be removed by
means of chemical transport reactions with good reproducibility, so that the
electric conductivity of the sheath can be easily adjusted by appropriate
control of the reaction.
Basically, for carrying out the method the superconductor to be
treated along with a transport agent need only be placed in an evacuated or
a protective gas filled reaction vessel and the vessel then heated to get the
chomical transport reaction. Evon if the conductor and the wall of the vessel
are at the same temperature, the element to be removed of the compound will
still be transported from the conductor sheath to the wall of the reaction
vessel, where it then precipitates as a met~llic mirror~ Such a transport
of matter without a temperature gradient suprisingly has been found possible
since even at an even temperature different reaction equilibria evidently
adjust themselves in the two corresponding transport reactions ~cEurri~t
the alloy forming the source for the element to be transported and at the
wall of the vessel.
It is particularly advantageous, however, to not precipitate the
element to be removed at the wall of the vessel, but to provide a suitable
gette~ in the viCin;ty of the super conductor to be treated for the element
to be removed. Preferably, the getter will consist of the electrically
highly norm~l conducting metal which is also contained in the alloy. The
getter advantageously will concentrically surround the conductor.
It is further advisable to establish a temperature gradient between
the conductor and the getter to accelerate the transport reaction. As a
rule, the conductor is kept at a higher temperature, and the getter at a
lswsr tomperature.
For stabilizing a conductor with at lea~t one core which consists
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entirely or partl~ of Nb3Sn and is surrounded by a copper-tin ~lloy, it haq
been found particularly advantageous to subject the conductor to an annealing
treatment in an hydrogen cEloride gas atmosphere in the presence of a copper
gotter, since chlorine or hydrogen chloride is a particularly good transport
agent for tin, The conductor will advantageously be kept in the temperature
range of 700 to 800C, with the temperature of the getter about 10 to 40C
lower than the temperature of the conductor,
For stabili~ing a conductor with at least one core which consists
entirely or partly of V3Ga and i9 surrounded by a copper-gallium alloy, the
process is similar. Preferably, iodine rather than chlorine will be used
since iodine is particularly well suited as a transport agent for gallium,
The single figure schematically illustrates an apparatus for
carrying out the method of the present invention.
ExamDlo 1
A pioce about 15 cm long of a ribbon shaped conductor, 440 ~m wide
and 100 ~m thick, with 220 cores of Nb3Sn embedded in a copper_tin matrix
was subjected to a chemical transport reaction to lower the tin content of
tho matrix. For this purpose, the conductor section was placed in a quartz
ampoulo about 12 cm long with an inside diameter o~ about 30~m~. A copper
wire approximatel~ 10 cm long and with a diamoter of about 500 ~m was also
placod in the ampoule for use as the getter material. Thereupon the ampoule
was evacuated down to a residual gas pressure of 10 6Torr, was then filled
~ith hydrogon chloride gas with a pressure of 0.05 Torr at room temperature,
and was soaled. The ampoulo was then heated for 48 hours with the ribbon
shapod conductor hold at a temperature of about 750C and the copper wire
serving as tho getter material at a temperaturo of about 730C. Subsequently,
tho ampoulo wa~ coolod down and opened.
A motallographic examination of samples of the treated conductor
boforo and after tho removal of tho tin from the matrix by the chemical trans-
port reaction ~howed a distinct color difference in the two samples. Prior to
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the transport reaction the wire sample was yellow, i.e., the color of
bronze, and after the transport reaction, definitely copper colored Measure-
ment of the residual resistance of samples before and after the transport
reaction show~d a value of l.S X 10 ohm cm before and a v~lue of 1.5X 10-6
ohm cm after i.e., a reduction by a factor 10 of the residual resistance
because of the chemical transport reaction The tin concentrations in the
alloy matrix of the conductor, which were determined by microprobe mea~urement,
were about 6.3 atom percent of tin before the transport reaction and about
0 3 atom percent of tin after the transport reaction.
Thus, the method according to the present invention is extremely
well suited for removing the tin from the copper tin matrix of a finished
conductor with diffused Nb3Sn cores and producing a low resistance copper
matrix.
Exam~le 2
The apparatus shown in the figure is particularly well suited for
treating longer wires using the method of the present invention. The super-
conductor 1 to be treated, e.g., an Nb Sn multi-core conductor with a copper_
tin matrix, is first wouhd on a ceramic tube 2. The tube 2 is placed in a
quartz ampoule 3 and pushod on a re-entrant part 4 provided in the ampoule.
A copper tube S is inserted into the ampoule for use as the getter in such
a manner that it concentric~lly surrounds the cera~ic tube 2 wo~nd with the
wire 1, The ampoule is evacuated down to about 10~6Torr and filled with
hydrogen chloride gas to a pressure of 0.05 Torr. The superconducting wire
1 i9 then heated to a temperature of about 750C, with a heater finger 6
placod in the ro-onb~ring part 4 and the tubular getter 5 heated with a tube
fu~naoo 7 to a temperature of about 740C. As at the surface of the tin
rich matrix of the wire 1 the equilibrium of the transport reaction is shift-
ed toward the formation of tin chloride, and at the tin poor surface of the
getter 5, it is shifted toward the liberation of tin, i.e., tin is trans-
orted from the wire 1 to tho getter 5 by the chemical transport reaction.
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The method according to the present invention can be applied to
all superconductors with superconductive intermetallic compound~ regardless
of their specific preparation, as long as they have a sheath of an alloy
of an electrically highly conductive metal and a chemical, transportable
element. These and other modifications may be made without departing from
the spirit of the invention which is intended to be limited solely by the
appended claims,
